The PA said she had never seen a facial CMN before so she wanted to get the doctor. I was completely fine with that and was prepared for it. The doctor was really nice, and said while she has not seen many cases of a facial CMN she had seen them. This was no surprise because it's rare, so there aren't many to see.
The doctor was impressed with her surgery and said we had a very skilled plastic surgeon. She was however concerned with one area by her lip that is so much darker than the rest of the nevus and wants a biopsy done. Haleigh would need to be put to sleep for the biopsy, which they do not do there. They recommended us to a plastic surgery center here in town, but said we might be happier with the doctor we already had.
It was time to call Atlanta.
Haliegh with her cousins. |
Everyone there is so understanding. I was told they would be able to do the biopsy with her next surgery. Because of the scheduling problems we have been having needing a biopsy is a blessing and a worry all in one. It puts Haleigh surgery from a elective to a need, so schedules will not be as big as a problem. This is a huge blessing, but the fact that she even needs a biopsy is a huge worry for me. We always put sunscreen on her, but the fact remains that her chance of cancer is still greater than mine. That's the part I hate. I will handle everything else, but I don't want handle that not now not ever. But we also know God has a plan and through Him all things are possible.
I should be hearing when her surgery is after Thanksgiving. The dermatologist sent Atlanta a letter along with the picture with the darker spots circled. After Atlanta receives this we will be scheduled.
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